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Class II: temporary or reversible health riskTerminated

Cantrell Drug Ephedrine Sulfate in 0 Recall

Ephedrine Sulfate in 0

Cantrell Drug Company · Little Rock, AR

Risk level
Class II
Reported by FDA
Aug 16, 2017
Recall ID
D-1064-2017
Check your lot numberHow we source this data

Summary

Cantrell Drug recalled Ephedrine Sulfate in 0 starting Jul 14, 2017. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1064-2017 on Aug 16, 2017. Reason: Lack of Sterility Assurance. Status: Terminated.

Why it was recalled

Lack of Sterility Assurance.

Product description

Ephedrine Sulfate in 0.9% Sodium Chloride 5 mL, 50 mg/5 mL (10 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222, NDC 52533-118-15

Lot numbers, UPCs & expiration codes

Lot #: 9904, 9914, 9939, BUD: 7/28/2017; 9952, 9969, 10004, BUD: 8/4/2017; 10043, 10088, 10115, BUD: 8/17/2017; 10269, BUD: 9/8/2017;10431, BUD: 9/23/2017; 10554, BUD: 10/27/2017

Where it was sold

Nationwide within the US

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1064-2017
Classification
Class II
Status
Terminated
Recall initiated
Jul 14, 2017
FDA report date
Aug 16, 2017
Quantity
49666 syringes
Recall type
Voluntary: Firm initiated
Recalling firm
Cantrell Drug Company

Original FDA data

Every field from FDA enforcement report D-1064-2017, exactly as published.

Show all FDA fields
City
Little Rock
State
AR
Status
Terminated
Country
United States
Event ID
77780
Address
7321 Cantrell Rd
Code information
Lot #: 9904, 9914, 9939, BUD: 7/28/2017; 9952, 9969, 10004, BUD: 8/4/2017; 10043, 10088, 10115, BUD: 8/17/2017; 10269, BUD: 9/8/2017;10431, BUD: 9/23/2017; 10554, BUD: 10/27/2017
Postal code
72207-4144
Report date
Aug 16, 2017
Product type
Drugs
Recall number
D-1064-2017
Classification
Class II
Recalling firm
Cantrell Drug Company
Product quantity
49666 syringes
Termination date
Sep 16, 2020
Reason for recall
Lack of Sterility Assurance.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Ephedrine Sulfate in 0.9% Sodium Chloride 5 mL, 50 mg/5 mL (10 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222, NDC 52533-118-15
Distribution pattern
Nationwide within the US
Recall initiation date
Jul 14, 2017
Initial firm notification
Letter
Center classification date
Aug 9, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1064-2017, published Aug 16, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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